Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNKS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9679968:9679968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012G>A
AA Mutation	p.Glu338Lys(p.E338K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9556289:9556289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350C>A
AA Mutation	p.Ala117Asp(p.A117D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9730963:9730963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2075C>T
AA Mutation	p.Ala692Val(p.A692V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9556564:9556564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Ala209Thr(p.A209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9720399:9720399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1775A>G
AA Mutation	p.Gln592Arg(p.Q592R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9752621:9752621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3148G>A
AA Mutation	p.Glu1050Lys(p.E1050K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9770215:9770215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762090867
CDS Mutation	c.3850G>A
AA Mutation	p.Val1284Ile(p.V1284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9556571:9556571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632A>G
AA Mutation	p.Asp211Gly(p.D211G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9556572:9556572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633C>G
AA Mutation	p.Asp211Glu(p.D211E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310430
Start	9751609:9751609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2833G>A
AA Mutation	p.Ala945Thr(p.A945T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9748127:9748127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2747C>T
AA Mutation	p.Thr916Met(p.T916M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310430
Start	9766424:9766424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3739A>G
AA Mutation	p.Arg1247Gly(p.R1247G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9748193:9748193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756350259
CDS Mutation	c.2813C>T
AA Mutation	p.Thr938Met(p.T938M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9751650:9751650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200640807
CDS Mutation	c.2874A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9735453:9735453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2610T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9556287:9556287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9706828:9706828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9708471:9708471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370231803
CDS Mutation	c.1557G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310430
Start	9556140:9556140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310430
Start	9708430:9708430(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1522delA
AA Mutation	p.Thr508HisfsTer33(p.T508Hfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000310430
Start	9704702:9704702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747680650
CDS Mutation	c.1147C>T
AA Mutation	p.Arg383Ter(p.R383*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000310430
Start	9556174:9556174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
AA Mutation	p.Arg79Ter(p.R79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000310430
Start	9776664:9776664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3912T>A
AA Mutation	p.Tyr1304Ter(p.Y1304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310430
Start	9710033:9710034(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1664dupA
AA Mutation	p.Asn555LysfsTer2(p.N555Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TNKS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9770243:9770243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3878T>A
AA Mutation	p.Val1293Asp(p.V1293D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9726677:9726677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1958G>A
AA Mutation	p.Arg653Gln(p.R653Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310430
Start	9766421:9766421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3736C>T
AA Mutation	p.His1246Tyr(p.H1246Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310430
Start	9710034:9710034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1664delA
AA Mutation	p.Asn555IlefsTer5(p.N555Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript